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Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling
Existing normative flow cytometry data have several limitations including small sample sizes, incompletely described study populations, variable flow cytometry methodology, and limited depth for defining lymphocyte subpopulations. To overcome these issues, we defined high-dimensional flow cytometry...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905525/ https://www.ncbi.nlm.nih.gov/pubmed/31825961 http://dx.doi.org/10.1371/journal.pone.0225512 |
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author | Yi, John S. Rosa-Bray, Marilyn Staats, Janet Zakroysky, Pearl Chan, Cliburn Russo, Melissa A. Dumbauld, Chelsae White, Scott Gierman, Todd Weinhold, Kent J. Guptill, Jeffrey T. |
author_facet | Yi, John S. Rosa-Bray, Marilyn Staats, Janet Zakroysky, Pearl Chan, Cliburn Russo, Melissa A. Dumbauld, Chelsae White, Scott Gierman, Todd Weinhold, Kent J. Guptill, Jeffrey T. |
author_sort | Yi, John S. |
collection | PubMed |
description | Existing normative flow cytometry data have several limitations including small sample sizes, incompletely described study populations, variable flow cytometry methodology, and limited depth for defining lymphocyte subpopulations. To overcome these issues, we defined high-dimensional flow cytometry reference ranges for the healthy human immune system using Human Immunology Project Consortium methodologies after carefully screening 127 subjects deemed healthy through clinical and laboratory testing. We enrolled subjects in the following age cohorts: 18–29 years, 30–39, 40–49, and 50–66 and enrolled cohorts to ensure an even gender distribution and at least 30% non-Caucasians. From peripheral blood mononuclear cells, flow cytometry reference ranges were defined for >50 immune subsets including T-cell (activation, maturation, T follicular helper and regulatory T cell), B-cell, and innate cells. We also developed a web tool for visualization of the dataset and download of raw data. This dataset provides the immunology community with a resource to compare and extract data from rigorously characterized healthy subjects across age groups, gender and race. |
format | Online Article Text |
id | pubmed-6905525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69055252019-12-27 Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling Yi, John S. Rosa-Bray, Marilyn Staats, Janet Zakroysky, Pearl Chan, Cliburn Russo, Melissa A. Dumbauld, Chelsae White, Scott Gierman, Todd Weinhold, Kent J. Guptill, Jeffrey T. PLoS One Research Article Existing normative flow cytometry data have several limitations including small sample sizes, incompletely described study populations, variable flow cytometry methodology, and limited depth for defining lymphocyte subpopulations. To overcome these issues, we defined high-dimensional flow cytometry reference ranges for the healthy human immune system using Human Immunology Project Consortium methodologies after carefully screening 127 subjects deemed healthy through clinical and laboratory testing. We enrolled subjects in the following age cohorts: 18–29 years, 30–39, 40–49, and 50–66 and enrolled cohorts to ensure an even gender distribution and at least 30% non-Caucasians. From peripheral blood mononuclear cells, flow cytometry reference ranges were defined for >50 immune subsets including T-cell (activation, maturation, T follicular helper and regulatory T cell), B-cell, and innate cells. We also developed a web tool for visualization of the dataset and download of raw data. This dataset provides the immunology community with a resource to compare and extract data from rigorously characterized healthy subjects across age groups, gender and race. Public Library of Science 2019-12-11 /pmc/articles/PMC6905525/ /pubmed/31825961 http://dx.doi.org/10.1371/journal.pone.0225512 Text en © 2019 Yi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Yi, John S. Rosa-Bray, Marilyn Staats, Janet Zakroysky, Pearl Chan, Cliburn Russo, Melissa A. Dumbauld, Chelsae White, Scott Gierman, Todd Weinhold, Kent J. Guptill, Jeffrey T. Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling |
title | Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling |
title_full | Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling |
title_fullStr | Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling |
title_full_unstemmed | Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling |
title_short | Establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling |
title_sort | establishment of normative ranges of the healthy human immune system with comprehensive polychromatic flow cytometry profiling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905525/ https://www.ncbi.nlm.nih.gov/pubmed/31825961 http://dx.doi.org/10.1371/journal.pone.0225512 |
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